| High rate of recurrent de novo mutations in developmental and epileptic encephalopathies FF Hamdan, CT Myers, P Cossette, P Lemay, D Spiegelman, AD Laporte, ... The American Journal of Human Genetics 101 (5), 664-685, 2017 | 399 | 2017 |
| The cell-intrinsic requirement of Sox6 for cortical interneuron development R Batista-Brito, E Rossignol, J Hjerling-Leffler, M Denaxa, M Wegner, ... Neuron 63 (4), 466-481, 2009 | 231 | 2009 |
| Genetics and function of neocortical GABAergic interneurons in neurodevelopmental disorders E Rossignol Neural plasticity 2011, 2011 | 207 | 2011 |
| The genetic landscape of infantile spasms JL Michaud, M Lachance, FF Hamdan, L Carmant, A Lortie, P Diadori, ... Human molecular genetics 23 (18), 4846-4858, 2014 | 198 | 2014 |
| CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms L Damaj, A Lupien-Meilleur, A Lortie, É Riou, LH Ospina, L Gagnon, ... European Journal of Human Genetics 23 (11), 1505-1512, 2015 | 195 | 2015 |
| Satb1 is an activity-modulated transcription factor required for the terminal differentiation and connectivity of medial ganglionic eminence-derived cortical interneurons J Close, H Xu, NDM García, R Batista-Brito, E Rossignol, B Rudy, ... Journal of Neuroscience 32 (49), 17690-17705, 2012 | 148 | 2012 |
| De novo mutations in the motor domain of KIF1A cause cognitive impairment, spastic paraparesis, axonal neuropathy, and cerebellar atrophy JR Lee, M Srour, D Kim, FF Hamdan, SH Lim, C Brunel‐Guitton, ... Human mutation 36 (1), 69-78, 2015 | 135 | 2015 |
| Recessive mutations in VPS13D cause childhood onset movement disorders J Gauthier, IA Meijer, D Lessel, NE Mencacci, D Krainc, M Hempel, ... Annals of neurology 83 (6), 1089-1095, 2018 | 123 | 2018 |
| CaV2.1 ablation in cortical interneurons selectively impairs fast‐spiking basket cells and causes generalized seizures E Rossignol, I Kruglikov, AMJM Van Den Maagdenberg, B Rudy, G Fishell Annals of neurology 74 (2), 209-222, 2013 | 118 | 2013 |
| Involvement of cortical fast-spiking parvalbumin-positive basket cells in epilepsy X Jiang, M Lachance, E Rossignol Progress in brain research 226, 81-126, 2016 | 102 | 2016 |
| Vagus nerve stimulation in pediatric epileptic syndromes E Rossignol, A Lortie, T Thomas, A Bouthiller, D Scavarda, C Mercier, ... Seizure 18 (1), 34-37, 2009 | 102 | 2009 |
| Natural history of vanishing white matter EMC Hamilton, HDW van der Lei, G Vermeulen, JAM Gerver, ... Annals of neurology 84 (2), 274-288, 2018 | 97 | 2018 |
| Opposing regulation of dopaminergic activity and exploratory motor behavior by forebrain and brainstem cholinergic circuits JC Patel, E Rossignol, ME Rice, RP Machold Nature communications 3 (1), 1172, 2012 | 88 | 2012 |
| Both gain‐of‐function and loss‐of‐function de novo CACNA1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox … X Jiang, PK Raju, N D'Avanzo, M Lachance, J Pepin, F Dubeau, ... Epilepsia 60 (9), 1881-1894, 2019 | 74 | 2019 |
| Mutations in ACTL6B cause neurodevelopmental deficits and epilepsy and lead to loss of dendrites in human neurons S Bell, J Rousseau, H Peng, Z Aouabed, P Priam, JF Theroux, M Jefri, ... The American Journal of Human Genetics 104 (5), 815-834, 2019 | 74 | 2019 |
| Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-Canadians N Dupré, N Chrestian, JP Bouchard, E Rossignol, D Brunet, D Sternberg, ... Neuromuscular Disorders 19 (5), 330-334, 2009 | 74 | 2009 |
| Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness I Perrault, FF Hamdan, M Rio, JM Capo-Chichi, N Boddaert, JC Décarie, ... The American Journal of Human Genetics 94 (6), 891-897, 2014 | 64 | 2014 |
| Evolution and treatment of childhood chronic inflammatory polyneuropathy E Rossignol, G D’Anjou, N Lapointe, E Haddad, M Vanasse Pediatric neurology 36 (2), 88-94, 2007 | 58 | 2007 |
| IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients C Mignot, AC McMahon, C Bar, PM Campeau, C Davidson, J Buratti, ... Genetics in Medicine 21 (4), 837-849, 2019 | 57 | 2019 |
| A Gain‐of‐Function Mutation in NALCN in a Child with Intellectual Disability, Ataxia, and Arthrogryposis K Aoyagi, E Rossignol, FF Hamdan, B Mulcahy, L Xie, S Nagamatsu, ... Human Mutation 36 (8), 753-757, 2015 | 54 | 2015 |
Jean-Claude LacailleDept Neurosciences, Université de MontréalAdresse e-mail validée de umontreal.ca
